PtBr2-Catalyzed Transformation of Allyl(o-ethynylaryl)carbinol

Journal of the American Chemical Society 2012 134 (21), 8762-8765 ... Pd(0)-Catalyzed [1,5]-Sigmatropic Hydrogen Shift of Propargylic Esters toward ...
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PtBr2-Catalyzed Transformation of Allyl(o-ethynylaryl)carbinol Derivatives into Functionalized Indenes. Formal sp3 C-H Bond Activation Gan B. Bajracharya, Nirmal K. Pahadi, Ilya D. Gridnev, and Yoshinori Yamamoto* Department of Chemistry, Graduate School of Science, Tohoku UniVersity, Sendai 980-8578, Japan [email protected] ReceiVed May 8, 2006

The PtBr2-catalyzed reaction of 1-ethynyl-2-(1-alkoxybut-3-enyl)benzenes at 120 °C in CH3CN gave functionalized indenes in good to allowable yields. Most probably, the hydrogen at the terminal alkyne is transferred to the adjacent internal β-carbon to form an (η2-vinylidene)platinum carbene intermediate, which activates the sp3 C-H bond at the benzylic carbon. This reaction pathway is supported by DFT calculations which suggest that the formation of the Pt-vinylidene complex is the rate-limiting stage for the whole transformation.

Introduction Transition-metal-catalyzed cyclization of alkynes for the synthesis of carbo- and heterocycles has attracted great attention in recent years.1 Although it is well established that terminal alkynes on treatment with transition metals lead to the formation of (η2-vinylidene)metal complexes, we still await further development of synthetically useful transformations through these intermediates.2 Depending upon the type of involved nucleophiles, mechanistically two distinct classes of intramolecular cycloisomerizations through metal vinylidene complexes exist in the literature: (1) intramolecular cyclization of dienylalkynes through 6π-electrocyclization (eq 1)3 and (2) cyclization of terminal alkynes tethered to hetero- and carbonucleophiles (eq 2).2e In the latter case, a stoichiometric amount of a base is needed to remove a proton from YH. It is rather surprising that carbon nucleophiles have not been explored in the line of this strategy, except for in McDonald’s paper.4 Herein, we report the PtBr2-catalyzed transformation of 1-ethynyl-2-(1-alkoxybut-3-enyl)benzenes 1 into functionalized indenes 2 in which most probably a formal sp3 C-H activation takes place by carbene insertion into the C-H bond of the Pt-vinylidene complex (eq 3).2f,5 We recently reported forma(1) For recent reviews see: (a) Nakamura, I.; Yamamoto, Y. Chem. ReV. 2004, 104, 2127. (b) Zeni, G.; Larock, R. C. Chem. ReV. 2004, 104, 2285. (c) Takacs, J. M.; Vayalakkada, S.; Jiang, X. Science of Synthesis; Thieme: Stuttgart, Germany, 2003; Vol. 1, pp 265-318.

tion of 1-vinylnaphthalenes 4 in the PtBr2-catalyzed reaction of the internal alkyne analogues 3, in which the cyclobutene intermediates are formed through Pt-catalyzed enyne metathesis (eq 4).6 It is interesting that the terminal alkynes 1 behaved differently. (2) For reviews, see: (a) Bruce, M. I.; Swincer, A. G. AdV. Organomet. Chem. 1983, 22, 59. (b) Bruce, M. I. Chem. ReV. 1991, 91, 197. (c) Bruneau, C.; Dixneuf, P. H. Acc. Chem. Res. 1999, 32, 311. Also see: (d) Weyerhausen, B.; Dotz, K. H. Eur. J. Inorg. Chem. 1999, 1057. (e) McDonald, F. E. Chem.sEur. J. 1999, 5, 3103 and references therein. (f) Nevado, C.; Echavarren, A. M. Synthesis 2005, 167 and references therein. (g) Miki, K.; Uemura, S.; Ohe, K. Chem. Lett. 2005, 34, 1068 and references therein. (3) (a) Merlic, C. A.; Pauly, M. E. J. Am. Chem. Soc. 1996, 118, 11319. Also see: (b) Miura, T.; Iwasawa, N. J. Am. Chem. Soc. 2002, 124, 518 and references therein. (c) Dankwardt, J. W. Tetrahedron Lett. 2001, 42, 5809. (d) Martı´n-Matute, B.; Nevado, C.; Ca´rdenas, D. J.; Echavarren, A. M. J. Am. Chem. Soc. 2003, 125, 5757. (e) Madhushaw, R. J.; Lo, C.-Y.; Hwang, C.-W.; Su, M.-D.; Shen, H.-C.; Pal, S.; Shaikh, I. R.; Liu, R.-S. J. Am. Chem. Soc. 2004, 126, 15560 and references therein. (4) McDonald, F. E.; Olson, T. C. Tetrahedron Lett. 1997, 38, 7691. NaH (0.5 equiv) was used as a base, and 0.5 equiv of (Et3N)Mo(CO)5 was needed to promote the carbocyclization. (5) (a) Recently, ruthenium vinylidene complex-mediated alkenylation of pyridine at the R-C-H bond via [2 + 2] heterocycloaddition was reported: Murakami, M.; Hori, S. J. Am. Chem. Soc. 2003, 125, 4720. For recent advances in C-H activation, see: (b) Handbook of C-H Transformation, Applications in Organic Synthesis; Dyker, G., Ed.; Wiley-VCH: Weinheim, 2005; Vols. 1 and 2. (6) Bajracharya, G. B.; Nakamura, I.; Yamamoto, Y. J. Org. Chem. 2005, 70, 892. 10.1021/jo060951g CCC: $33.50 © 2006 American Chemical Society

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Published on Web 07/14/2006

Allyl(ethynylaryl)carbinol Transformation into Indenes

Results and Discussion In our initial experimental setup, when 1-ethynyl-2-(1-methoxybut-3-enyl)benzene (1a) was heated with 2 mol % PtBr2 in 1,4-dioxane at 120 °C for 42 h, 1-allyl-1-methoxy-1H-indene (2a) was isolated in 42% yield as the major product together with 24% 1-vinylnaphthalene (4a) (R ) H). Encouraged by this result, we further optimized the reaction conditions. When CH3CN was used as solvent, the selectivity for the formation of 2a was improved. Increasing the amount of catalyst loading (5 mol %) was proved worthy, and 2a was isolated in 55% yield in 12 h (65% NMR yield) (Table 1, entry 1). Besides platinum halides, [RuCl2(CO)3]2 could be used as an alternative catalyst,7 but it requires a longer reaction time. Other catalysts, such as NiBr2, PdCl2(CH3CN)2, Pd(PPh3)4, Rh6(CO)16, CoCl2, W(CO)6, AuCl3, etc., did not promote the reaction at all. This reaction was not sensitive to moisture and was unaffected by addition of 50 mol % H2O. The reaction was completely halted on treatment with an additional base (e.g., K2CO3 and Et3N). Olefin additives, such as β-pinene (which can activate the platinum catalyst through π-coordination),8 produced a comparable yield. The scope of this reaction is summarized in Table 1. The reaction of substrates 1b-d proceeded smoothly, affording the (7) More recently, two papers on cycloisomerization via Ru- and Rhvinylidene intermediates appeared: (a) Datta, S.; Odedra, A.; Liu, R.-S. J. Am. Chem. Soc. 2005, 127, 11606. (b) Kim, H.; Lee, C. J. Am. Chem. Soc. 2005, 127, 10180. (8) Recently, we reported the Pd-catalyzed carbocyclization of alkynylacetals in which the cleavage of the C-O bond of o-alkynylbenzaldehyde acetal produces the cationic intermediate and both the triple bond and the acetal group are bonded to the metal. Ring closure of the cationic intermediates leads to the cyclic vinyl cations, which are trapped by PdOR. (a) Nakamura, I.; Bajracharya, G. B.; Wu, H.; Oishi, K.; Mizushima, Y.; Gridnev, I. D.; Yamamoto, Y. J. Am. Chem. Soc. 2004, 126, 15423. (b) Nakamura, I.; Bajracharya, G. B.; Yamamoto, Y. Chem. Lett. 2005, 34, 174. (c) Nakamura, I.; Mizushima, Y.; Gridnev, I. D.; Yamamoto, Y. J. Am. Chem. Soc. 2005, 127, 9844. We were aware that if the present reaction proceeds through a similar mechanistic fashion, 7a, 7b, 7c, or 7d should be obtained. None of them were obtained.

corresponding indene derivatives 2b-d with a high selectivity over the formation of 4a (entries 2-4). No significant effect was observed with the bulkiness of the alkoxide moiety. The reaction of 1e,f bearing an electron-donating substituent (OMe) at the aromatic ring proceeded with perfect selectivity and produced the corresponding products 2e,f (entries 5 and 6). Similarly, an excellent selectivity was observed with the substrate 1g bearing a poor electron-withdrawing group (F) under the standard conditions, and product 2g was isolated in a moderate yield (entry 7). On the other hand, the presence of a strong electron-withdrawing group (CF3) reduced both the chemical yield and selectivity (entries 8 and 9). We tested the effect of the R1 group in 1 on the present carbocyclization. The saturated analogue 1j, the vinyl derivative 1k bearing a shorter carbon chain, and 1l having a longer carbon chain did not give 2 at all under the standard conditions; decomposition of the substrates took place, and a complex mixture of products was obtained. This observation suggests that the coordination of olefin to Pt at a right position/geometry might be essential for the indene formation. External olefin additives did not exert an influence on the reaction, but the internal olefin was needed to induce the reaction. On the other hand, replacing the methoxy substituent with the phenyl group proved to be possible. Thus, the phenyl-substituted analogue 1-ethynyl-2-(1-phenylbut-3-enyl)benzene (5) gave 1-allyl-1phenyl-1H-indene (6) in 40% isolated yield (eq 5).

A deuterium-labeling experiment was carried out to get additional data for the elucidation of the reaction mechanism. When the substrate 1a-d was treated with 5 mol % PtBr2 under the standard conditions, the corresponding product 2a-d (labeled with 100% deuterium at C-2 position) was obtained in 50% yield (eq 6). The deuterium labeling at another position was

not observed. The structure of 2a-d, as well as perfect selectivity of the position of deuterium incorporation, strongly suggests the intermediate formation of a vinylidene intermediate similar to those shown in eqs 1 and 2. In the case of a cationic pathway similar to the cyclization reactions of o-alkynylbenzaldehyde acetals and thioacetals,8 one would expect some randomness in the distribution of deuterium. Moreover, the cationic mechanism would open the door to the migration of the methoxy group, actually observed in the corresponding reactions but not in the reaction under study. This observation corresponds well to the mechanism involving vinylidene insertion into the C-H bond, since it implies the conservation of the C-OMe bond throughout the whole transformation (Scheme 1). Another argument for the intermediate vinylidene formation in the case of terminal acetylenes is the completely different structure of the products yielded by the alkyl-substituted substrates under the same conditions (eq 4).6 Although we are unaware of known examples J. Org. Chem, Vol. 71, No. 16, 2006 6205

Bajracharya et al. TABLE 1. PtBr2-Catalyzed endo-Carbocyclization of Terminal Alkynesa

a Conditions: 5 mol % PtBr , CH CN, 120 °C, 12 h. b Combined yields of 2 + 4 based on 1H NMR analysis; isolated yields are in parentheses. c Ratio 2 3 based on isolated yield. d Reaction time was 24 h.

of platinum vinylidene intermediates, recent results demonstrate that the pincer vinylidene complexes of Pt(IV) can be isolated.9 To get more support for the mechanism of Pt-vinylidene insertion, we have followed the reaction pathway (Scheme 1) computationally (Figures 1 and 2).We have located the structures of three different complexes of PtBr2 with the starting compound 1a, viz., alkyne-PtBr2-alkene complex 7, PtBr2-vinylidene complex 8, alkyne-PtBr2-OMe complex 9, and PtBr2-product complex 10 (Scheme 1, Figure 2). Interestingly, PtBr2-vinylidene complex 8 is much more stable (about 8 kcal/mol) than alkyne-PtBr2-OMe complex 9 and only 2.2 kcal/mol less stable than starting 7. The geometry of the Pt atom in 8 is very close to square planar (angles 6206 J. Org. Chem., Vol. 71, No. 16, 2006

Br-Pt-Br and Br-Pt-C are 91.6° and 82.5°, respectively). On the other hand, in the optimized structure of the intermediate 11 (analogue of 8 having a vinyl substituent instead of allyl) the square planar geometry of Pt atom is significantly distorted (angles Br-Pt-Br and Br-Pt-C are 104.5° and 49.1°, respectively). The less effective intramolecular coordination of the vinyl substituent might be one of the reasons why we failed to obtain the corresponding cyclization products, although one cannot exclude the possibility of just inferior stability of the vinyl-substituted product. (9) Kubo, K.; Jones, D.; Ferguson, M. J.; McDonald, R.; Cavell, R. G. J. Am. Chem. Soc. 2005, 127, 5314.

Allyl(ethynylaryl)carbinol Transformation into Indenes SCHEME 1.

Formation of the Product via Insertion of the PtBr2-Vinylidene Complex into the C-Hb Bond

We have also located transition structures (Figure 3) connecting 7 and 8 (TS1) as well as 8 and 10 (TS2); their validity was confirmed with the frequency analysis (only one negative vibration for either TS1 or TS2). In both transition structures the participation of the double bond in the Pt coordination is evident: the Pt atom keeps almost ideal square planar geometry, one of the four ligands being the double bond of the allylic substituent. The activation barrier for the isomerization of 7 to 8 is quite high (33.4 kcal/mol); this is the limiting stage of the whole transformation, since the activation barrier of the cyclization step is quite low (3.1 kcal/mol). Energy minimization using TS2 as the input structure afforded 10; therefore, no other intermediates are involved in the cyclization step. A alternative transition state (TS3) for the limiting stage connecting 9 and 12 (analogue of 8 with Pt coordinated to OR rather than to the double bond) was also computed. It was 18.2 kcal/mol higher in energy than TS1. The geometry of the Pt atom in TS3 strongly deviated from square planar. Hence, the computational results indicate that the uniqueness of the allyl-

substituted substrates for the cyclization might be stipulated for the geometry of the allylic substituent which is appropriate to keep the square planar geometry on the Pt atom throughout the whole transformation. Experimental Section General Information. 1H NMR spectra are reported as follows: chemical shift in parts per million (δ) relative to the chemical shift of CDCl3 at 7.24 ppm, integration, multiplicities (s ) singlet, d ) doublet, t ) triplet, m ) multiplet), and coupling constants (Hz). 13C NMR spectra are reported in parts per million (δ) relative to the central line of the triplet for CDCl3 at 77 ppm. IR bands are reported in inverse centimeters. Column chromatography was carried out employing silica gel 60 N (spherical, neutral, 100-210 µm). Analytical thin-layer chromatography (TLC) was performed on 0.2 mm precoated plate Kieselgel 60 F254. All manipulations were conducted under an argon atmosphere using standard Schlenk techniques. Materials. 2-[(Trimethylsilanyl)ethynyl]benzaldehyde derivatives were obtained from the coupling of the corresponding 2-bromoben-

FIGURE 1. Energy profile for the transformation of the alkyne-Pt-alkene complex 7 to the product-PtBr2 complex 10. J. Org. Chem, Vol. 71, No. 16, 2006 6207

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FIGURE 2. Structures of Pt complexes 7-10 optimized at the B3LYP/ SDD level of theory. The relative energies are given with respect to product-PtB2 complex 10.

FIGURE 3. Transition structures TS1 and TS2 optimized at the B3LYP/SDD level of theory via the QST3 procedure. The relative energies are given with respect to product-PtB2 complex 10.

zaldehyde derivatives with (trimethylsilyl)acetylene by using the Sonogashira reaction.10 2-[(Trimethylsilanyl)ethynyl]benzaldehyde derivatives were then treated with KF in methanol for the deprotection of the trimethylsilyl group, producing the corresponding 2-ethynylbenzaldehydes. 2-Ethynylbenzaldehydes on treatment with allyltrimethylsilane in the presence of scandium triflate following the known protocol produced the desired 1-ethynyl-2(1-alkoxybut-3-enyl)benzene.11 2-Bromobenzaldehyde, 2-bromo(10) For a review, see: Brandsma, L.; Vasilevsky, S. F.; Verkruijsse, H. D. Application of Transition Metal Catalyst in Organic Synthesis; Springer-Verlag: Berlin, Heidelberg, 1999; Chapter 10. (11) Yadav, J. S.; Subba Reddy, B. V.; Srihari, P. Synlett 2001, 673.

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5-fluorobenzaldehyde, (trimethylsilyl)acetylene, and allyltrimethylsilane were purchased and used as received. 2-Bromo-5-methoxybenzaldehyde,12 2-bromo-4-methoxybenzaldehyde,13 2-bromo4-(trifluoromethyl)benzaldehyde,14 and 2-bromo-5-(trifluoromethyl)benzaldehyde14 were prepared according to the reported procedures. 2-[(Trimethylsilanyl)ethynyl]benzaldehyde on treatment with phenylmagnesium bromide produced phenyl[2-[(trimethylsilanyl)ethynyl]phenyl]methanol, which after allylation15 followed by deprotection of the trimethylsilyl group using KF afforded 1-ethynyl-2(1-phenylbut-3-enyl)benzene. All the catalysts used were commercially available. Representative Procedure for the endo-Carbocyclization. To a mixture of PtBr2 (5.3 mg, 0.015 mmol, 5 mol %) and 1-ethynyl2-(1-methoxybut-3-enyl)benzene (1a) (55.9 mg, 0.3 mmol) was added CH3CN (5.0 mL, 0.06 M) under an argon atmosphere in a microreactor. The mixture was stirred for 20 min at room temperature and then heated at 120 °C for 12 h. The product was filtered through a short column of SiO2 using ethyl acetate as an eluent, and the resulting filtrate was concentrated. The residue was purified by column chromatography (silica gel, hexane/ethyl acetate, 100/1) to afford 1-allyl-1-methoxy-1H-indene (2a) in 55% yield (30.7 mg), and 1-vinylnaphthalene (4a) was obtained in 6% yield (2.8 mg). Data for 1-allyl-1-methoxy-1H-indene (2a): Rf 0.52 (silica gel, hexane/EtOAc, 10/1); 1H NMR (500 MHz, CDCl3) δ 2.52 (dd, J ) 7.0, 14.0 Hz, 1H), 2.71 (dd, J ) 7.5, 14.0 Hz, 1H), 2.97 (s, 3H), 5.02-4.98 (m, 2H), 5.77-5.69 (m, 1H), 6.19 (d, J ) 5.5 Hz, 1H), 6.74 (d, J ) 5.5 Hz, 1H), 7.32-7.18 (m, 4H); 13C NMR (125 MHz, CDCl3) δ 42.2, 51.7, 89.7, 117.7, 121.5, 122.6, 126.0, 128.5, 132.9, 133.7, 139.3, 143.0, 145.0; IR (neat) 3070-2824, 1640, 1464, 1315, 1101, 1074, 990, 920, 791, 758 cm-1; HRMS (EI) m/z calcd for C13H14O (M+) 186.1045, found 186.1039. Anal. Calcd for C13H14O (186.25): C, 83.83; H, 7.58. Found: C, 83.54; H, 7.66. The structure of 2a was confirmed by an NOE experiment:

Data for 1-allyl-1-ethoxy-1H-indene (2b): Rf 0.48 (silica gel, hexane/EtOAc, 10/1); yield 53%; 1H NMR (400 MHz, CDCl3) δ 0.99 (t, J ) 7.2 Hz, 3H), 2.45 (dd, J ) 7.2, 14.0 Hz, 1H), 2.64 (dd, J ) 7.2, 14.0 Hz, 1H), 2.96-2.88 (m, 1H), 3.17-3.10 (m, 1H), 4.91-4.86 (m, 2H), 5.66-5.57 (m, 1H), 6.13 (d, J ) 5.6 Hz, 1H), 6.62 (d, J ) 5.6 Hz, 1H), 7.25-7.08 (m, 4H); 13C NMR (100 MHz, CDCl3) δ 16.0, 42.3, 59.2, 89.2, 117.4, 121.2, 122.5, 125.8, 128.2, 132.1, 133.6, 139.9, 142.7, 145.7; IR (neat) 3070-2876, 1639, 1464, 1456, 1315, 1119, 1080, 995, 914, 789, 756 cm-1; HRMS (EI) m/z calcd for C14H16O (M+) 200.1201, found 200.1204. Anal. Calcd for C14H16O (200.28): C, 83.96; H, 8.05. Found: C, 84.09; H, 7.72. Data for 1-allyl-1-butoxy-1H-indene (2c): Rf 0.44 (silica gel, hexane/EtOAc, 10/1); yield 50%; 1H NMR (400 MHz, CDCl3) δ (12) Gies, A.-E.; Pfeffer, M. J. Org. Chem. 1999, 64, 3650. (13) Stuffert, J.; Abraham, E.; Raeppel, S.; Bruˆckner, R. V. Liebigs Ann. 1996, 447. (14) (a) Sˇ indela´rˇ, K.; Dlabacˇ, A.; Metysˇova´, J.; Kaka´cˇ, B.; Holubek, J.; Sva´tek, E.; Sedivy´, Z.; Protiva, M. Collect. Czech. Chem. Commun. 1975, 40, 1940. (b) Perchonock, C. D.; Uzinskas, I.; McCarthy, M. E.; Erhard, K. F.; Gleason, J. G.; Wasserman, M. A.; Muccitelli, R. M.; DeVan, J. F.; Tucker, S. S.; Vickery, L. M.; Kirchner, T.;. Weichman, B. M.; Mong, S.; Scott, M. O.; Chi-Rosso, G.; Wu, H.-L.; Croole, S. T.; Newton, J. F. J. Med. Chem. 1986, 29, 1442. (15) Yasuda, M.; Saito, T.; Ueba, M.; Baba, A. Angew. Chem., Int. Ed. 2004, 43, 1414.

Allyl(ethynylaryl)carbinol Transformation into Indenes 0.82 (t, J ) 7.2 Hz, 3H), 1.29-1.23 (m, 2H), 1.42-1.37 (m, 2H), 2.49 (dd, J ) 7.2, 13.6 Hz, 1H), 2.69 (dd, J ) 7.2, 13.6 Hz, 1H), 2.92 (td, J ) 6.8, 8.8 Hz, 1H), 3.12 (td, J ) 6.4, 9.2 Hz, 1H), 4.97-4.92 (m, 2H), 5.73-5.65 (m, 1H), 6.19 (d, J ) 6.0 Hz, 1H), 6.68 (d, J ) 6.0 Hz, 1H), 7.30-7.14 (m, 4H); 13C NMR (100 MHz, CDCl3) δ 14.0, 19.3, 32.5, 42.4, 63.4, 89.0, 117.3, 121.2, 122.5, 125.7, 128.2, 132.1, 133.7, 140.0, 142.7, 145.7; IR (neat) 30702870, 1639, 1464, 1315, 1281, 1094, 993, 914, 789, 756 cm-1; HRMS (EI) m/z calcd for C16H20O (M+) 228.1514, found 228.1514. Anal. Calcd for C16H20O (228.33): C, 84.16; H, 8.83. Found: C, 84.29; H, 8.92. Data for 1-allyl-1-benzyloxy-1H-indene (2d): Rf 0.38 (silica gel, hexane/EtOAc, 10/1); yield 49%; 1H NMR (400 MHz, CDCl3) δ 2.58 (dd, J ) 7.2, 13.6 Hz, 1H), 2.79 (dd, J ) 7.2, 13.6 Hz, 1H), 4.02 (d, J ) 11.6 Hz, 1H), 4.18 (d, J ) 11.6 Hz, 1H), 5.01-4.96 (m, 2H), 5.83-5.73 (m, 1H), 6.25 (d, J ) 5.6 Hz, 1H), 6.74 (d, J ) 5.6 Hz, 1H), 7.38-7.17 (m, 9H); 13C NMR (100 MHz, CDCl3) δ 42.3, 65.7, 89.5, 117.6, 121.4, 122.7, 126.0, 127.1, 127.2, 128.1, 128.4, 132.6, 133.6, 139.3, 139.5, 142.8, 145.2; IR (neat) 30672860, 1637, 1558, 1497, 1456, 1379, 1317, 1097, 1063, 993, 916, 756 cm-1; HRMS (EI) m/z calcd for C19H18O (M+) 262.1358, found 262.1359. Anal. Calcd for C19H18O (262.35): C, 86.99; H, 6.92. Found: C, 86.67; H, 7.15. Data for 1-allyl-1,6-dimethoxy-1H-indene (2e): Rf 0.55 (silica gel, hexane/EtOAc, 8/2); yield 65%; 1H NMR (400 MHz, CDCl3) δ 2.48 (dd, J ) 7.2, 14.0 Hz, 1H), 2.67 (dd, J ) 7.2, 14.0 Hz, 1H), 2.96 (s, 3H), 3.81 (s, 3H), 5.03-4.97 (m, 2H), 5.76-5.66 (m, 1H), 6.06 (d, J ) 5.6 Hz, 1H), 6.66 (d, J ) 5.6 Hz, 1H), 6.76-6.74 (m, 1H), 6.91-6.89 (m, 1H), 7.09-7.07 (m, 1H); 13C NMR (100 MHz, CDCl3) δ 42.6, 51.7, 55.5, 89.6, 109.7, 112.8, 117.6, 121.7, 132.4, 133.5, 135.6, 137.0, 147.0, 158.7; IR (neat) 3074-2825, 1599, 1475, 1429, 1364, 1313, 1279, 1161, 1101, 1068, 1030, 916, 816, 781 cm-1; HRMS (EI) m/z calcd for C14H16O2 (M+) 216.1150, found 216.1150. Anal. Calcd for C14H16O2 (216.28): C, 77.75; H, 7.46. Found: C, 77.60; H, 7.35. Data for 1-allyl-1,5-dimethoxy-1H-indene (2f): Rf 0.31 (silica gel, hexane/EtOAc, 10/1); yield 20%; 1H NMR (400 MHz, CDCl3) δ 2.50 (dd, J ) 7.2, 14.0 Hz, 1H), 2.66 (dd, J ) 7.2, 14.0 Hz, 1H), 2.94 (s, 3H), 3.80 (s, 3H), 5.01-4.96 (m, 2H), 5.76-5.66 (m, 1H), 6.19 (d, J ) 5.6 Hz, 1H), 6.66 (d, J ) 5.6 Hz, 1H), 6.70-6.68 (m, 1H), 6.77-6.75 (m, 1H), 7.19-7.16 (m, 1H); 13C NMR (100 MHz, CDCl3) δ 42.3, 51.5, 55.4, 89.0, 108.0, 110.4, 117.6, 123.2, 132.5, 133.7, 136.6, 140.5, 144.5, 160.2; IR (neat) 3072-2833, 1610, 1508, 1473, 1431, 1279, 1257, 1232, 1032, 916, 831, 787 cm-1; GC-MS m/z calcd for C14H16O2 (M+) 216.1, found 216.0. Anal. Calcd for C14H16O2 (216.28): C, 77.75; H, 7.46. Found: C, 78.02; H, 7.07. Data for 1-allyl-6-fluoro-1-methoxy-1H-indene (2g): Rf 0.40 (silica gel, hexane/EtOAc, 10/1); yield 50%; 1H NMR (400 MHz, CDCl3) δ 2.48 (dd, J ) 7.2, 14.0 Hz, 1H), 2.65 (dd, J ) 7.2, 14.0 Hz, 1H), 2.96 (s, 3H), 5.02-4.96 (m, 2H), 5.74-5.64 (m, 1H), 6.16 (d, J ) 5.6 Hz, 1H), 6.67 (d, J ) 5.6 Hz, 1H), 6.94-6.89 (m, 1H), 7.03-7.00 (m, 1H), 7.12-7.09 (m, 1H); 13C NMR (100 MHz, CDCl3) δ 42.2, 51.8, 89.6, 110.8, 114.8, 118.0, 122.0, 132.0, 133.1, 138.7, 147.6, 160.8, 163.5; IR (neat) 3076-2825, 1641, 1603, 1472, 1427, 1362, 1257, 1101, 987, 912, 872, 825, 783, 739 cm-1; HRMS (EI) m/z calcd for C13H13FO (M+) 204.0950, found 204.0952. Anal. Calcd for C13H13FO (204.24): C, 76.45; H, 6.42; F, 9.30. Found: C, 76.34; H, 6.64. Data for 1-allyl-1-methoxy-5-(trifluoromethyl)-1H-indene (2h): Rf 0.42 (silica gel, hexane/EtOAc, 10/1); yield 21%; 1H NMR (400 MHz, CDCl3) δ 2.51 (dd, J ) 7.2, 14.0 Hz, 1H), 2.67 (dd, J ) 7.2, 14.0 Hz, 1H), 2.95 (s, 3H), 5.00-4.96 (m, 2H), 5.75-5.65 (m, 1H), 6.30 (d, J ) 5.6 Hz, 1H), 6.75 (d, J ) 5.6 Hz, 1H), 7.477.38 (m, 3H); 13C NMR (100 MHz, CDCl3) δ 42.0, 52.0, 90.0, 118.2, 118.2, 122.7, 123.1, 130.7, 131.0, 131.9, 132.9, 141.1, 143.4, 148.8; IR (neat) 3078-2827, 1431, 1360, 1321, 1269, 1165, 1126, 1076, 1053, 920, 895, 837, 791, 746 cm-1; GC-MS m/z calcd for

C14H13F3O (M+) 254.1, found 254.0. Anal. Calcd for C14H13F3O (254.25): C, 66.14; H, 5.15; F, 22.42. Found: C, 66.17; H, 5.36. Data for 1-allyl-1-methoxy-6-(trifluoromethyl)-1H-indene (2i): Rf 0.42 (silica gel, hexane/EtOAc, 10/1); yield 9%; 1H NMR (400 MHz, CDCl3) δ 2.51 (dd, J ) 7.2, 14.0 Hz, 1H), 2.68 (dd, J ) 7.2, 14.0 Hz, 1H), 2.96 (s, 3H), 5.01-4.96 (m, 2H), 5.75-5.65 (m, 1H), 6.36 (d, J ) 5.6 Hz, 1H), 6.75 (d, J ) 5.6 Hz, 1H), 7.287.26 (m, 1H), 7.53-7.51 (m, 2H); 13C NMR (100 MHz, CDCl3) δ 42.0, 52.0, 90.0, 117.3, 118.3, 119.3, 121.4, 126.0, 126.1, 131.9, 132.9, 142.4, 145.7, 146.2; IR (neat) 3076-2827, 1431, 1331, 1267, 1165, 1122, 1076, 1053, 918, 839 cm-1; GC-MS m/z calcd for C14H13F3O (M+) 254.1, found 254.0. Anal. Calcd for C14H13F3O (254.25): C, 66.14; H, 5.15; F, 22.42. Found: C, 66.41; H, 5.28. Data for 1-vinylnaphthalene (4a):16Rf 0.66 (silica gel, hexane/ EtOAc, 10/1); 1H NMR (400 MHz, CDCl3) δ 5.48 (dd, J ) 1.6, 10.8 Hz, 1H), 5.80 (dd, J ) 1.6, 17.2 Hz, 1H), 7.54-7.40 (m, 4H), 7.64-7.62 (m, 1H), 7.87-7.78 (m, 2H), 8.15-8.11 (m, 1H); 13C NMR (100 MHz, CDCl3) δ 117.0, 123.5, 123.7, 125.5, 125.7, 126.0, 128.0, 128.4, 131.0, 133.5, 134.3, 135.5; IR (neat) 3085-2978, 1618, 1590, 1509, 1418, 1389, 1341, 1168, 1009, 986, 916, 861, 800, 777 cm-1; GC-MS m/z calcd for C12H10 (M+) 154.1, found 154.0. Data for 7-(trifluoromethyl)-1-vinylnaphthalene (4b): Rf 0.58 (silica gel, hexane/EtOAc, 10/1); yield 15%; 1H NMR (400 MHz, CDCl3) δ 5.55 (dd, J ) 1.2, 10.8 Hz, 1H), 5.81 (dd, J ) 1.2, 17.2 Hz, 1H), 7.48-7.41 (m, 1H), 7.58-7.54 (m, 1H), 7.70-7.63 (m, 2H), 7.83-7.81 (m, 1H), 7.95-7.93 (m, 1H), 8.438.37 (m, 1H); 13C NMR (100 MHz, CDCl3) δ 118.4, 121.3, 121.7, 124.8, 125.8, 127.5, 127.8, 127.8, 129.5, 129.9, 133.5, 134.7, 136.6; IR (neat) 3090-2924, 1462, 1313, 1234, 1161, 1122, 1068, 837, 754, 739 cm-1; GC-MS m/z calcd for C13H9F3 (M+) 122.1, found 122.0. Data for 6-(trifluoromethyl)-1-vinylnaphthalene (4c): Rf 0.62 (silica gel, hexane/EtOAc, 10/1); yield 16%; 1H NMR (400 MHz, CDCl3) δ 5.53 (dd, J ) 1.2, 11.2 Hz, 1H), 5.80 (dd, J ) 1.2, 17.2 Hz, 1H), 7.73-7.40 (m, 4H), 7.86-7.84 (m, 1H), 8.22-8.13 (m, 2H); 13C NMR (100 MHz, CDCl3) δ 118.1, 121.5, 121.5, 125.0, 125.7, 126.1, 126.9, 127.4, 128.1, 128.7, 132.3, 133.6, 135.8; IR (neat) 3088-2926, 1473, 1381, 1346, 1315, 1234, 1198, 1124, 1074, 918, 899, 831, 798, 758, 739 cm-1; GC-MS m/z calcd for C13H9F3 (M+) 122.1, found 122.0. Data for 1-allyl-1-phenyl-1H-indene (6): yellow liquid; 1H NMR (400 MHz, CDCl3) δ 2.84 (dd, J ) 6.8, 14.0 Hz, 1H), 3.05 (dd, J ) 7.6, 14.0 Hz, 1H), 4.99-4.94 (m, 1H), 4.89-4.85 (m, 1H), 5.49-5.42 (m, 1H), 6.55 (d, J ) 5.6 Hz, 1H), 6.78 (d, J ) 5.6 Hz, 1H), 7.32-7.12 (m, 10H); 13C NMR (100 MHz, CDCl3) δ 41.0, 60.6, 117.3, 121.4, 123.3, 125.3, 126.3, 126.5, 126.8, 128.4, 130.0, 134.3, 141.6, 143.4, 144.2, 150.7; IR (neat) 3062-2923, 1654, 1496, 1461, 1033, 914 cm-1; HRMS (EI) m/z calcd for C18H6 (M+) 232.1252, found 232.1250. Deuterium-Labeling Experiment. To a mixture of PtBr2 (5.3 mg, 0.015 mmol, 5 mol %) and 1-ethynyl-2-(1-deuterio-1-methoxybut-3-enyl)benzene (1a-d) (56.4 mg, 0.3 mmol) was added CH3CN (5.0 mL, 0.06 M) under an argon atmosphere in a microreactor. The mixture was stirred for 20 min at room temperature and then heated at 120 °C for 12 h. The product was filtered through a short column of SiO2 using ethyl acetate as an eluent, and the resulting filtrate was concentrated. The residue was purified by column chromatography (silica gel, hexane/ethyl acetate, 100/1) to afford 2a-d in 50% yield (28.1 mg), and 4a-d was obtained in 6% isolated yield (2.7 mg). Computational Details. Geometries of all stationary points were optimized using analytical energy gradients of self-consistent-field theory and density functional theory (DFT).17 The latter utilized Becke’s three-parameter exchange-correlation functional18 including the nonlocal gradient corrections described by Lee-Yang-Parr (16) Littke, A. F.; Schwarz, L.; Fu, G. C. J. Am. Chem. Soc. 2002, 124, 6343.

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Bajracharya et al. (LYP),19 as implemented in the Gaussian 03 program package.20 All geometry optimizations were performed using the SDD basis set.21 This approach is widely used for the recent computational studies of transition-metal complexes and was shown to yield results conforming with experimental data in our work8,22 and the work of others.23

Acknowledgment. The computational results in this research were obtained using supercomputing resources at the Information Synergy Center, Tohoku University. (17) (a) Parr, R. G.; Yang, W. Density Functional Theory of Atoms and Molecules; Oxford University Press: New York, 1989. (b) Cheeseman, J. R.; Frisch, M. J.; Devlin, F. J.; Stephens, P. J. Chem. Phys. Lett. 2 1996, 52, 211. (18) (a) Becke, A. D. Phys. ReV. A 1988, 38, 3098. (b) Becke, A. D. J. Chem. Phys. 1993, 98, 5648. (19) (a) Lee, C.; Yang, W.; Parr, R. G. Phys. ReV. B 1988, 37, 785. (b) Miehlich, B.; Savin, A.; Stoll, H.; Preuss, H. Chem. Phys. Lett. 1989, 157, 200.

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Supporting Information Available: NMR charts, Cartesian Coordinates, and full Gaussian citation. This material is available free of charge via the Internet at http://pubs.acs.org. JO060951G (20) Gaussian 03, Revision B.05: M. J. Frisch et al., Gaussian, Inc., Pittsburgh PA, 2003 (full reference in the Supporting Information). (21) (a) Dunning, T. H., Jr.; Hay, P. J. In Modern Theoretical Chemistry; Schaefer, H. F., III, Ed.; Plenum: New York, 1976; Vol. 3, p 1. (b) Leininger, T.; Nicklass, A.; Stoll, H.; Dolg, M.; Schwerdtfeger, P. J. Chem. Phys. 1996, 105, 1052. (22) (a) Nishikata, T.; Yamamoto, Y.; Gridnev, I. D.; Miyaura, N. Organometallics 2005, 25, 5025. (b) Gridnev, I. D.; del Rosario, M. K. C.; Zhanpeisov, N. U. J. Phys. Chem. B 2005, 109, 12498. (c) Imamoto, T.; Yashio, K.; Crepy, K. V. L.; Katagiri, K.; Takahashi, H.; Kouchi, M.; Gridnev, I. D. Organometallics 2006, 26, 908. (d) Patil, N. T.; Lutete, L. M.; Wu, H.; Pahadi, N. K.; Gridnev, I. D.; Yamamoto, Y. J. Org. Chem. 2006, 71, 4270. (23) (a) Bittner, M.; Koppel, H. J. Phys. Chem. A 2004, 108, 11116. (b) McKee, M. L.; Swart, M. Inorg. Chem. 2005, 44, 6975. (c) Kondo, T.; Tsunawaki, F.; Ura, Y.; Sadaoka, K.; Iwasa, T.; Wada, K.; Mitsudo, T. Organometallics 2005, 24, 905. (d) Nowroozi-Isfahani, T.; Musaev, D. G.; McDonald, F. E.; Morokuma, K. Organometallics 2005, 24, 2921.